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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201673Generated: October 29, 2026

Potassium Carbonate → tert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamate

https://huagongshe.com/reaction/2201673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactanttert-Butyl (4-bromo-2-nitrophenyl)carbamateHCID 52904808—
CatalystHCID 178418397HCID 178418397—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Producttert-Butyl 2-nitro-4-(thiophen-2-yl)phenylcarbamateHCID 5973698473%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of tert-butyl (4-bromo-2-nitrophenyl)carbamate (6.0 g, 18.92 mmol, 1.0 eq.), thiophen-2-ylboronic acid (3.2 g, 24.6 mmol, 1.3 eq.), potassium carbonate (7.84 g, 56.8 mmol, 3.0 eq.) and tetrakis(triphenylphosphine)palladium(0) (1.53 g, 1.32 mmol, 0.07 eq.), tri-tolylphosphine in DME/H2O (105 mL) was first degassed then heated to 90° C. for 20 h. The reaction was then filtered through Celite. The product was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by flash column chromatography (silica gel, 2% EtOAc/hexanes) to obtain pure tert-butyl (2-nitro-4-(thiophen-2-yl)phenyl)carbamate (4.42 g, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365498B2
Source datasetuspto-grants-2016_06
ORD IDord-056071ab81bc45fe893c3e68d40e7d74
Source noteuspto-grants-2016_06